Biosimilars Uptake & Patient Safety

Biosimilar engineers and their outsourcing accomplices must know about the picked nation's administrative scene, and have broad information of any current biosimilar endorsement pathway and the most recent administrative organization rules. Furnishing administrative experts with endorsements of investigation (CoA) for a U.S.- advertised comparator could challenge. As opposed to European practice, U.S. makers tend not to make CoAs accessible to parties required in the production network or bolster the improvement of a contender by discharging CoAs for clumps acquired for clinical trials. Giving family proclamations to the reference item more often than not is acknowledged as an option.

  • Case studies of biosimilar approvals/rejections
  • Challenges in clinical development
  • Analytical Development and Quality Control

Related Conference of Biosimilars Uptake & Patient Safety

November 09-11, 2017

4th European Biopharma Congress

Vienna, Austria
August 20-22, 2018

9th Asian Biologics and Biosimilars Congress

Tokyo, Japan

Biosimilars Uptake & Patient Safety Conference Speakers

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